Label: SOLEIL FORTE MULTI- octinoxate, octisalate, homosalate, avobenzone, octocrylene lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 69769-101-11, 69769-101-51 - Packager: LINEX HEALTH & BEAUTY
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 29, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENTS
WATER, CYCLOPENTASILOXANE, GLYCERIN, PEG-10 DIMETHICONE, POLYMETHYL METHACRYLATE, DIMETHICONE, CETEARYL ISONONANOATE, METHYL METHACRYLATE CROSSPOLYMER, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, POLYGLYCERYL-3 POLYRICINOLEATE, ACRYLATES/DIMETHICONE COPOLYMER, SODIUM CHLORIDE, GINKGO BILOBA LEAF EXTRACT, JOJOBA ESTERS, ALOE BARBADENSIS LEAF JUICE, PHENOXYETHANOL, DISTEARDIMONIUM HECTORITE, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, BUTYLENE GLYCOL, SORBITAN SESQUIOLEATE, CETYL RICINOLEATE, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, GLYCERYL CAPRATE, MAGNESIUM STEARATE, ALUMINUM TRISTEARATE, SILICA SILYLATE, HEXYLENE GLYCOL, TOCOPHEROL, BEESWAX, VINYL DIMETHICONE/METHICONE SESQUIOXANE CROSSPOLYMER, LYCIUM BARBARUM FRUIT EXTRACT, FRAGRANCE.
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOLEIL FORTE MULTI
octinoxate, octisalate, homosalate, avobenzone, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69769-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 5 g in 100 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2.75 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) .ALPHA.,.BETA.'-DIGLYCERIN (UNII: LG6U99J4V1) POLYGLYCEROL POLYRICINOLEIC ACID (UNII: 3C96Y1D5T4) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) SODIUM CHLORIDE (UNII: 451W47IQ8X) GINKGO BILOBA WHOLE (UNII: 660486U6OI) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) ALOE VERA LEAF (UNII: ZY81Z83H0X) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CETYL RICINOLEATE (UNII: 1P677500YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERYL CAPRATE (UNII: 197M6VFC1W) MAGNESIUM STEARATE (UNII: 70097M6I30) ALUMINUM STEARATES (UNII: O4D7U3B46U) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) HEXYLENE GLYCOL (UNII: KEH0A3F75J) TOCOPHEROL (UNII: R0ZB2556P8) YELLOW WAX (UNII: 2ZA36H0S2V) POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK) LYCIUM BARBARUM FRUIT (UNII: 930626MWDL) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) CETEARYL ISONONANOATE (UNII: P5O01U99NI) METHYL METHACRYLATE (UNII: 196OC77688) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69769-101-51 1 in 1 BOX 04/24/2015 1 NDC:69769-101-11 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/24/2015 Labeler - LINEX HEALTH & BEAUTY (050219996)